6-Azaindazole
1H-pyrazolo[3,4-c]pyridine
CAS: 271-47-6
Molecular Formula: C6H5N3
6-Azaindazole - Names and Identifiers
| Name | 1H-pyrazolo[3,4-c]pyridine |
| Synonyms | 6-Azaindazole 6-Aza-1H-indazole 1H-pyrazolo[3,4-c]pyridine 1H-PYRAZOLO[3,4-C]PYRIDINE 1H-Pyrazolo(3,4-c)pyridine |
| CAS | 271-47-6 |
| InChI | InChI=1/C6H5N3/c1-2-7-4-6-5(1)3-8-9-6/h1-4H,(H,8,9) |
6-Azaindazole - Physico-chemical Properties
| Molecular Formula | C6H5N3 |
| Molar Mass | 119.12 |
| Density | 1.348±0.06 g/cm3 (20 ºC 760 Torr) |
| Boling Point | 318.8±15.0 °C(Predicted) |
| Flash Point | 161°C |
| Vapor Presure | 0.00066mmHg at 25°C |
| pKa | 10.94±0.30(Predicted) |
| Storage Condition | Inert atmosphere,Room Temperature |
| Refractive Index | 1.715 |
| MDL | MFCD00661308 |
6-Azaindazole - Risk and Safety
| Hazard Symbols | Xn - Harmful |
| Risk Codes | 22 - Harmful if swallowed |
6-Azaindazole - Introduction
1H-pyrazolo[3,4-c]pyridine is an aromatic compound with the formula C8H6N2. It has the appearance of a white or off-white crystalline powder.
The compound is commonly used as an intermediate in organic synthesis and is widely used in the manufacture of drugs and pesticides. It can also be used as a precursor for dyes and pigments, and as a material for organic light-emitting diodes (OLEDs).
The method for preparing 1H-pyrazolo[3,4-c]pyridine is usually obtained by the cycloaddition reaction of carbamate and 1,5-dibromopentane under alkaline conditions. Toxic gases may be generated during the reaction, so it is necessary to operate under well-ventilated conditions.
Regarding safety information, 1H-pyrazolo[3,4-c]pyridine is a chemical and should be properly disposed. When in use, should follow the relevant safety procedures, and wear appropriate protective equipment, such as safety glasses and gloves. During storage, keep away from fire and oxidizing agents, and keep the container sealed.
The compound is commonly used as an intermediate in organic synthesis and is widely used in the manufacture of drugs and pesticides. It can also be used as a precursor for dyes and pigments, and as a material for organic light-emitting diodes (OLEDs).
The method for preparing 1H-pyrazolo[3,4-c]pyridine is usually obtained by the cycloaddition reaction of carbamate and 1,5-dibromopentane under alkaline conditions. Toxic gases may be generated during the reaction, so it is necessary to operate under well-ventilated conditions.
Regarding safety information, 1H-pyrazolo[3,4-c]pyridine is a chemical and should be properly disposed. When in use, should follow the relevant safety procedures, and wear appropriate protective equipment, such as safety glasses and gloves. During storage, keep away from fire and oxidizing agents, and keep the container sealed.
Last Update：2024-04-09 20:49:11
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